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AAGTCATCAGCAACTCTGCTTCTGA[C/T]CTGGGGCCTGGAGGATGTGGAGCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602120 | ||||||||||||||||||||
Literature Links: |
CHD3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CHD3 - chromodomain helicase DNA binding protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005271.2 | 642 | Missense Mutation | ACC,ATC | T,I 200 | NP_001005271.2 | |
NM_001005273.2 | 642 | Missense Mutation | ACC,ATC | T,I 141 | NP_001005273.1 | |
NM_005852.3 | 642 | Missense Mutation | ACC,ATC | T,I 141 | NP_005843.2 | |
XM_005256427.4 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_005256484.1 | |
XM_005256428.4 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_005256485.1 | |
XM_005256429.4 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_005256486.1 | |
XM_005256431.4 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_005256488.1 | |
XM_006721423.3 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_006721486.1 | |
XM_006721424.3 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_006721487.1 | |
XM_006721428.3 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_006721491.1 | |
XM_017024061.1 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_016879550.1 | |
XM_017024062.1 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_016879551.1 | |
XM_017024063.1 | 642 | Missense Mutation | ACC,ATC | T,I 141 | XP_016879552.1 | |
XM_017024064.1 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_016879553.1 | |
XM_017024065.1 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_016879554.1 | |
XM_017024066.1 | 642 | Missense Mutation | ACC,ATC | T,I 121 | XP_016879555.1 | |
XM_017024067.1 | 642 | Missense Mutation | ACC,ATC | T,I 130 | XP_016879556.1 | |
XM_017024068.1 | 642 | Missense Mutation | ACC,ATC | T,I 121 | XP_016879557.1 | |
XM_017024069.1 | 642 | UTR 5 | XP_016879558.1 | |||
XM_017024070.1 | 642 | Missense Mutation | ACC,ATC | T,I 200 | XP_016879559.1 |
NAA38 - N(alpha)-acetyltransferase 38, NatC auxiliary subunit | ||||||
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There are no transcripts associated with this gene. |